A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089889



Internal ID21432886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63589845..63589845hg38UCSC Ensembl
chr15:63882044..63882044hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655937
Supporting Variants
SamplesHG00731
Known GenesUSP3, USP3-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089889
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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